A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2580n100



Internal ID20154196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41267962..41453282hg38UCSC Ensembl
chr15:41560160..41745480hg19UCSC Ensembl
chr15:39347452..39532772hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38185321
hg19185321
hg18185321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045142, nsv1044438
Samples
Known GenesCHP1, NDUFAF1, NUSAP1, OIP5, OIP5-AS1, RTF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2580n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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